scholarly journals Phosphaturic mesenchymal tumour: A rare tumour & its diagnostic dilemma

2020 ◽  
Vol 152 (7) ◽  
pp. 222
Author(s):  
SudhirKumar Srivastava ◽  
Aditya Raj
2015 ◽  
Vol 235 (4) ◽  
pp. 539-545 ◽  
Author(s):  
Jen-Chieh Lee ◽  
Yung-Ming Jeng ◽  
Sheng-Yao Su ◽  
Chen-Tu Wu ◽  
Keh-Sung Tsai ◽  
...  

2020 ◽  
Vol 90 (9) ◽  
pp. 1812-1814
Author(s):  
Jock Clarnette ◽  
Jakub Jagiello ◽  
Gelareh Farshid ◽  
Richard Smith

2020 ◽  
Vol 13 (11) ◽  
pp. e237678
Author(s):  
Laxman Pandey ◽  
Deepa Joseph ◽  
Rajesh Pasricha ◽  
Manoj Kumar Gupta

Primary synovial sarcoma of the lung (PSSL) is a rare tumour with only 0.5% incidence among other primary malignant lung tumours. Published medical literature regarding the natural history treatment protocol and clinical outcomes of PSSL remains limited. Here, we present a case of a 39-year-old man with primary synovial sarcoma with long-term follow-up, which was initially viewed as a metastasis from another unknown site. After evaluating histopathologically from the specimen post left lung metastasectomy and ruling out any other site for neoplastic changes, the diagnosis of PSSL was confirmed. Furthermore, this article reviews the literature and discusses various aspects of PSSL, including clinical presentation, radiological imaging and pathological characteristics, diagnostic dilemma, management and prognosis. This paper serves to provide an update and aims to enhance the understanding of PSSL. Timely diagnosis and treatment are imperative to achieve improved outcomes.


2016 ◽  
Vol 69 (11) ◽  
pp. 1037-1038 ◽  
Author(s):  
David Creytens ◽  
Jo Van Dorpe

Pathology ◽  
2014 ◽  
Vol 46 ◽  
pp. S76
Author(s):  
Archana Pandita ◽  
I. Kumarasamy ◽  
D. Kenwright

2012 ◽  
Vol 126 (7) ◽  
pp. 721-724 ◽  
Author(s):  
M I Syed ◽  
M Chatzimichalis ◽  
M Rössle ◽  
A M Huber

AbstractObjective:We describe the first reported case of a phosphaturic mesenchymal tumour, mixed connective tissue variant, invading the temporal bone.Case report:A female patient presented with increasing deafness. On examination there appeared to be a mass behind an intact tympanic membrane. Further radiological investigation showed a vascular mass occupying the middle ear, mastoid and internal auditory meatus. This was surgically resected and revealed to be a benign phosphaturic mesenchymal tumour, mixed connective tissue variant. The tumour recurred a year later, presenting as facial nerve palsy. A revision procedure was carried out; the tumour was excised with the sacrifice of a segment of the facial nerve, and a facial-hypoglossal nerve anastomosis was performed.Conclusion:This case report highlights the occurrence of this benign but sometimes aggressive tumour, of which both clinicians and pathologists should be aware. Early recognition of the condition remains of utmost importance to minimise the debilitating consequences of long-term osteomalacia in affected patients, and to prevent extracranial and intracranial complications caused by the tumour.


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